FDA NDC Directory · JSON-LD · Markdown

FAMOTIDINE

NDC 59651-701 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA219091
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsFAMOTIDINE (40 mg/5mL)
Marketing started20250709
Package count1

External sources

Source: openFDA. Public-domain (CC0).